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PGNM publications reflect the scientific output of the laboratory’s teams and collaborators, spanning fundamental mechanisms, disease models, technologies and translational research.

2023
Ilio Vitale, Federico Pietrocola, Emma Guilbaud, Stuart Aaronson, John Abrams, Dieter Adam, Massimil..., Apoptotic cell death in disease—Current understanding of the NCCD 2023, Cell Death and Differentiation.
2023
Alboni S, Secco V, Papotti B, Vilella A, Adorni MP, Zimetti F, Schaeffer L, Tascedda F, Zoli M, Lebl..., Hydroxypropyl-β-Cyclodextrin Depletes Membrane Cholesterol and Inhibits SARS-CoV-2 Entry into HEK293T-ACEhi Cells., Pathogens 2023 Apr; 12(5): .
2023
Jaque-Fernandez F, Allard B, Monteiro L, Lafoux A, Huchet C, Jaimovich E, Berthier C, Jacquemond V, Probenecid affects muscle Ca2+ homeostasis and contraction independently from pannexin channel block., J Gen Physiol 2023 Apr; 155(4): .
2023
Cikes D, Elsayad K, Sezgin E, Koitai E, Torma F, Orthofer M, Yarwood R, Heinz LX, Sedlyarov V, Miran..., Author Correction: PCYT2-regulated lipid biosynthesis is critical to muscle health and ageing., Nat Metab 2023 Apr; 5(4): 711.
2023
Cikes D, Elsayad K, Sezgin E, Koitai E, Torma F, Orthofer M, Yarwood R, Heinz LX, Sedlyarov V, Miran..., PCYT2-regulated lipid biosynthesis is critical to muscle health and ageing., Nat Metab 2023 Mar; 5(3): 495-515.
2023
Simon Roubille, Franceline Juillard, Tristan Escure, Olivier Binda, Armelle Corpet, Stuart Bloor, Ca..., The HUSH-SETDB1-MORC2 epigenetic repressor complex restricts herpesvirus infection in association with PML nuclear bodies, .
2023
Tahraoui-Bories J, Mérien A, González-Barriga A, Lainé J, Leteur C, Polvèche H, Carteron A, De L..., MBNL-dependent impaired development within the neuromuscular system in myotonic dystrophy type 1., Neuropathol Appl Neurobiol 2023 Feb; 49(1): e12876.
2023
Siouda M, Dujardin AD, Dekeyzer B, Schaeffer L, Mulligan P, Chromodomain on Y-like 2 (CDYL2) implicated in mitosis and genome stability regulation via interaction with CHAMP1 and POGZ., Cell Mol Life Sci 2023 Jan; 80(2): 47.
2023
Flavie Strappazzon, Habilitation à Diriger des Recherches L’autophagie sélective au coeur de la physiopathologie, .
2023
Szentesi P, Dienes B, Kutchukian C, Czirjak T, Buj-Bello A, Jacquemond V, Csernoch L, Disrupted T-tubular network accounts for asynchronous calcium release in MTM1-deficient skeletal muscle., J Physiol 2023 Jan; 601(1): 99-121.
2023
Clara Bernard, Charline Jomard, Bénédicte Chazaud, Julien Gondin, Kinetics of skeletal muscle regeneration after mild and severe muscle damage induced by electrically‐evoked lengthening contractions, FASEB Journal.
2023
Repellin M, Carton F, Boschi F, Galiè M, Perduca M, Calderan L, Jacquier A, Carras J, Schaeffer L, ..., Repurposing pentamidine using hyaluronic acid-based nanocarriers for skeletal muscle treatment in myotonic dystrophy., Nanomedicine 2023 Jan; 47(): 102623.
2023
Svahn J, Coudert L, Streichenberger N, Kraut A, Gravier-Dumonceau-Mazelier A, Rotard L, Calemard-Mic..., Immune-Mediated Rippling Muscle Disease Associated With Thymoma and Anti-MURC/Cavin-4 Autoantibodies., Neurol Neuroimmunol Neuroinflamm 2023 Jan; 10(1): .
2023
Shaqraa Musawi, Lise-Marie Donnio, Zehui Zhao, Charlène Magnani, Phoebe Rassinoux, Olivier Binda, J..., Nucleolar reorganization after cellular stress is orchestrated by SMN shuttling between nuclear compartments, Nat Commun 2023 Nov; 14(1): 7384.
2022
, Initial TK-deficient HSV-1 infection in the lip alters contralateral lip challenge immune dynamics, Sci Rep 2022 May; 12(1): 8489.
2022
Arnaud Jacquier, Julian Theuriet, Fanny Fontaine, Valentine Mosbach, Nicolas Lacoste, Shams Ribault,..., Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy, Brain - A Journal of Neurology.
2022
Jacquier A, Ribault S, Mendes M, Lacoste N, Risson V, Carras J, Latour P, Nadaj-Pakleza A, Stojkovic..., Expanding the phenotypic variability of MORC2 gene mutations: From Charcot-Marie-Tooth disease to late-onset pure motor neuropathy., Hum Mutat 2022 Dec; 43(12): 1898-1908.
2022
Osseni A, Schaeffer L, [HDAC6, a very specific deacetylase with a potential therapeutic role]., Med Sci (Paris) 2022 Dec; 38 Hors série n° 1(): 6-12.
2022
Pegat A, Streichenberger N, Lacoste N, Hermier M, Menassa R, Coudert L, Theuriet J, Froissart R, Ter..., Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy-Case Report., Genes (Basel) 2022 Nov; 13(12): .
2022
Osseni A, Ravel-Chapuis A, Belotti E, Scionti I, Gangloff YG, Moncollin V, Mazelin L, Mounier R, Leb..., Pharmacological inhibition of HDAC6 improves muscle phenotypes in dystrophin-deficient mice by downregulating TGF-β via Smad3 acetylation., Nat Commun 2022 Nov; 13(1): 7108.